Results 31 to 40 of about 22,467,747 (285)

Microarray analysis in the Archaeon Halobacterium salinarum strain R1 [PDF]

, 2007
Background: Phototrophy of the extremely halophilic archaeon Halobacterium salinarum was explored for decades. The research was mainly focused on the expression of bacteriorhodopsin and its functional properties.
Wende Andy, Welzl, G., Wende, Andy, Oesterhelt, Dieter, Wende, A., Markus Panhuysen, Panhuysen, Markus, Dieter Oesterhelt, Pfeiffer Friedhelm, Soppa, Jörg (Prof. Dr.), Jens Twellmeyer, Pfeiffer, F., Soppa Jörg, Pfeiffer, Friedhelm, Twellmeyer, Jens, Wolfertz, J., Zaigler, Alexander, Oesterhelt Dieter, Jörg Soppa, Wolfertz Jan, Zaigler Alexander, Welzl Gerhard, Andy Wende, Soppa, J., Zaigler, A., Alexander Zaigler, Wolfertz, Jan, Oesterhelt, D., Welzl, Gerhard, Friedhelm Pfeiffer, Panhuysen, M., Twellmeyer Jens, Gerhard Welzl, Jan Wolfertz, Panhuysen Markus, Twellmeyer, J.   +35 more
core   +1 more source

An Interstitial 4q Deletion with a Mosaic Complementary Ring Chromosome in a Child with Dysmorphism, Linear Skin Pigmentation, and Hepatomegaly

Case Reports in Genetics, 2017
Interstitial deletions of 4q are rarely reported, vary in size, and have limited genotype-phenotype correlations. Here, genome-wide array CGH analysis identified a 21.6 Mb region of copy number loss at 4q12-q21.1 in a patient diagnosed with dysmorphism ...
J. Carter, H. Brittain, D. Morrogh, N. Lench, J. J. Waters   +4 more
doaj   +1 more source

Stable transmission of complex chromosomal rearrangements involving chromosome 1q derived from constitutional chromoanagenesis

Molecular Cytogenetics, 2019
Background Chromoanagenesis events encompassing chromoanasynthesis, chromoplexy, and chromothripsis are described in cancers and can result in highly complex chromosomal rearrangements derived from ‘all-at-once’ catastrophic cellular events.
Mary A. Gudipati, Elizabeth Waters, Carol Greene, Nidhi Goel, Nicole L. Hoppman, Beth A. Pitel, Matthew R. Webley, Ying Zou   +7 more
doaj   +1 more source

Dynamic distribution of SeqA protein across the chromosome of Escherichia coli K-12 [PDF]

, 2010
The bacterial SeqA protein binds to hemi-methylated GATC sequences that arise in newly synthesized DNA upon passage of the replication machinery. In Escherichia coli K-12, the single replication origin oriC is a well-characterized target for SeqA, which ...
Stephen J. W. Busby, Nigel P. Dyer, Sascha Ott, Sánchez-Romero, María Antonia, Dyer, NP, Millard, AD, Sanchez-Romero, MA, María Antonia Sánchez-Romero, Busby, Stephen; id_orcid, Ott, S, Grainger, David, Dyer, Nigel, Millard, Andrew D., David C. Grainger, Ott, Sascha, Andrew D. Millard, Busby, S. (Stephen), Grainger, David C.   +17 more
core   +1 more source

EMMA 2-A MAGE-compliant system for the collaborative analysis and integration of microarray data [PDF]

, 2009
Dondrup M, Albaum S, Griebel T, et al. EMMA 2-A MAGE-compliant system for the collaborative analysis and integration of microarray data. BMC Bioinformatics.
Jünemann, Sebastian, Kahlke, Tim, Dondrup Michael, Christiane K Kleindt, Küster, Helge, Albaum, Stefan P, Goesmann, Alexander ; https://orcid.org/, Pühler Alfred, Heiko Neuweger, Runte Kai J, Mittard-Runte Virginie, Mertens, Dominik, Mittard-Runte, Virginie, Runte, Kaj J, Kuester, Helge, Henckel, Kolja, Linke Burkhard, Albaum, Stefan ; https://orcid.org/, Albaum, Stefan P., Tauch Andreas, Tim Kahlke, Goesmann Alexander, Pühler, Alfred ; https://orcid.org/, Goesmann, Alexander, Stefan P Albaum, Burkhard Linke, Kai J Runte, Helge Küster, Tauch, Andreas, Tille, Felix, Kleindt Christiane K, Virginie Mittard-Runte, Sebastian Jünemann, Küster Helge, Kolja Henckel, Griebel, Thasso, Kleindt, Christiane K., Kleindt, Christiane Katja, Griebel Thasso, Jünemann Sebastian, Neuweger Heiko, Alfred Pühler, Dondrup, Michael, Alexander Goesmann, Henckel Kolja, Kleindt, Christiane K, Andreas Tauch, Neuweger, Heiko, Linke, Burkhard, Dominik Mertens, Pühler, Alfred, Albaum Stefan P, Tille Felix, Kahlke Tim, Michael Dondrup, Thasso Griebel, Runte, Kai J., Felix Tille, Mertens Dominik   +58 more
core   +1 more source

Microarray Analysis of Rat Chromosome 2 Congenic Strains [PDF]

Hypertension, 2003
Human essential hypertension is a complex polygenic trait with underlying genetic components that remain unknown. The stroke-prone spontaneously hypertensive rat (SHRSP) is a model of human essential hypertension, and a number of reproducible blood pressure regulation quantitative trait loci have been found to map to rat chromosome
Martin W, McBride, Fiona J, Carr, Delyth, Graham, Niall H, Anderson, James S, Clark, Wai K, Lee, Fadi J, Charchar, M Julia, Brosnan, Anna F, Dominiczak   +8 more
openaire   +2 more sources

Information visualization for DNA microarray data analysis: A critical review [PDF]

, 2008
Graphical representation may provide effective means of making sense of the complexity and sheer volume of data produced by DNA microarray experiments that monitor the expression patterns of thousands of genes simultaneously.
Kuljis, J, Liu, X, Zhang, Leishi, Zhang, L, Kujis, J.N., Liu, Xiaohui   +5 more
core   +1 more source

Mosaic Tetrasomy of 9p24.3q21.11 postnatally identified in an infant born with multiple congenital malformations: a case report

BMC Pediatrics, 2018
Background Supernumerary Marker Chromosomes consist in structurally abnormal chromosomes, considered as an extra chromosome in which around 70% occur as a de novo event and about 30% of the cases are mosaic. Tetrasomy 9p is a rare chromosomal abnormality
Irene Plaza Pinto, Lysa Bernardes Minasi, Raphael Steckelberg, Claudio Carlos da Silva, Aparecido Divino da Cruz   +4 more
doaj   +1 more source

The impact of chromosomal microarray on clinical management: a retrospective analysis [PDF]

Genetics in Medicine, 2014
Chromosomal microarray has been widely adopted as the first-tier clinical test for individuals with multiple congenital anomalies, developmental delay, intellectual disability, and autism spectrum disorders. Although chromosomal microarray has been extensively shown to provide a higher diagnostic yield than conventional cytogenetic methods, some health
Lindsay B, Henderson, Carolyn D, Applegate, Elizabeth, Wohler, Molly B, Sheridan, Julie, Hoover-Fong, Denise A S, Batista   +5 more
openaire   +2 more sources

Autosomal chromosome microdeletions in three adolescent girls with premature ovarian insufficiency: a case report

The Turkish Journal of Pediatrics, 2022
Background. Premature ovarian insufficiency (POI) in the pediatric age group is most commonly related to X chromosome abnormalities such as Turner syndrome. Autosomal chromosome microdeletions in ovarian failure are relatively rare.
Ke Yuan, Minfei He, Yanlan Fang, Jianfang Zhu, Li Liang, Chunlin Wang   +5 more
doaj   +1 more source